Linked Data
ClinVar Variation Id:
2933692
ClinVar RCV Id:
RCV003793250
dbSNP Id:
rs770391394
ExAC:
19:13135873 C / T
gnomAD v2:
19-13135873-C-T
gnomAD v4:
19-13025059-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.13025059C>T , CM000681.2:g.13025059C>T | GRCh38 |
| NC_000019.9:g.13135873C>T , CM000681.1:g.13135873C>T | GRCh37 |
| NC_000019.8:g.12996873C>T | NCBI36 |
| NG_032925.2:g.34290C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358552.8:c.63C>T | ENSP00000351354.5:p.His21= | |
| ENST00000622520.2:c.63C>T | ENSP00000481181.2:p.His21= | |
| ENST00000592199.6:c.66C>T MANE Select | ENSP00000467512.1:p.His22= | |
| ENST00000676441.1:c.90C>T | ENSP00000502554.1:p.His30= | |
| ENST00000358552.7:c.75C>T | ENSP00000351354.4:p.His25= | |
| ENST00000360105.8:c.75C>T | ENSP00000353219.4:p.His25= | |
| ENST00000397661.6:c.66C>T | ENSP00000380781.2:p.His22= | |
| ENST00000585382.5:c.-76C>T | ENSP00000466605.1:n.-76C>T | |
| ENST00000585575.5:c.42C>T | ENSP00000468794.1:p.His14= | |
| ENST00000586797.5:c.77C>T | ENSP00000467536.1:p.Thr26Met | |
| ENST00000586873.1:c.-76C>T | ENSP00000468707.1:n.-76C>T | |
| ENST00000587260.1:c.63C>T | ENSP00000467785.1:p.His21= | |
| ENST00000587760.5:c.42C>T | ENSP00000466389.1:p.His14= | |
| ENST00000588228.5:c.-76C>T | ENSP00000466735.1:n.-76C>T | |
| ENST00000590027.1:c.-76C>T | ENSP00000465616.1:n.-76C>T | |
| ENST00000591028.1:c.114C>T | ENSP00000465094.1:p.His38= | |
| ENST00000592199.5:c.66C>T | ENSP00000467512.1:p.His22= | |
| NM_001271043.2:c.90C>T | NP_001257972.1:p.His30= | |
| NM_001271044.2:c.42C>T | NP_001257973.1:p.His14= | |
| NM_002501.3:c.66C>T | NP_002492.2:p.His22= | |
| XM_005259917.3:c.243C>T | XP_005259974.1:p.His81= | |
| XM_005259918.3:c.66C>T | XP_005259975.1:p.His22= | |
| XM_005259919.3:c.243C>T | XP_005259976.1:p.His81= | |
| XM_005259920.3:c.42C>T | XP_005259977.1:p.His14= | |
| XM_005259921.3:c.243C>T | XP_005259978.1:p.His81= | |
| XM_005259922.3:c.243C>T | XP_005259979.1:p.His81= | |
| XM_006722760.2:c.243C>T | XP_006722823.1:p.His81= | |
| XM_011528040.1:c.114C>T | XP_011526342.1:p.His38= | |
| NM_001365902.1:c.66C>T | NP_001352831.1:p.His22= | |
| NM_001365982.1:c.66C>T | NP_001352911.1:p.His22= | |
| NM_001365983.1:c.-76C>T | NP_001352912.1:n.-76C>T | |
| NM_001365984.1:c.63C>T | NP_001352913.1:p.His21= | |
| NM_001365985.1:c.63C>T | NP_001352914.1:p.His21= | |
| XM_005259917.4:c.243C>T | XP_005259974.1:p.His81= | |
| NM_001271044.3:c.42C>T | NP_001257973.1:p.His14= | |
| NM_001365902.2:c.66C>T | NP_001352831.1:p.His22= | |
| NM_001365982.2:c.66C>T | NP_001352911.1:p.His22= | |
| NM_001365983.2:c.-76C>T | NP_001352912.1:n.-76C>T | |
| NM_001365984.2:c.63C>T | NP_001352913.1:p.His21= | |
| NM_001365985.2:c.63C>T | NP_001352914.1:p.His21= | |
| NM_002501.4:c.66C>T | NP_002492.2:p.His22= | |
| NM_001365902.3:c.66C>T MANE Select | NP_001352831.1:p.His22= | |
| NM_001378404.1:c.42C>T | NP_001365333.1:p.His14= | |
| NM_001378405.1:c.114C>T | NP_001365334.1:p.His38= |