Linked Data
dbSNP Id:
rs2075192245
gnomAD v3:
19-41978190-G-T
gnomAD v4:
19-41978190-G-T
MyVariant Identifiers:
chr19:g.42482342G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41978190G>T , CM000681.2:g.41978190G>T | GRCh38 |
| NC_000019.9:g.42482342G>T , CM000681.1:g.42482342G>T | GRCh37 |
| NC_000019.8:g.47174182G>T | NCBI36 |
| NG_008015.1:g.21041C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545399.6:c.1806C>A | ENSP00000444688.1:p.Val602= | |
| ENST00000644613.1:c.1767C>A | ENSP00000494711.1:p.Val589= | |
| ENST00000648268.1:c.1767C>A MANE Select | ENSP00000498113.1:p.Val589= | |
| ENST00000302102.9:c.1767C>A | ENSP00000302397.5:p.Val589= | |
| ENST00000441343.5:c.1767C>A | ENSP00000411503.1:p.Val589= | |
| ENST00000543770.5:c.1800C>A | ENSP00000437577.1:p.Val600= | |
| ENST00000545399.5:c.1806C>A | ENSP00000444688.1:p.Val602= | |
| ENST00000602133.5:c.1677C>A | ENSP00000471581.1:p.Val559= | |
| NM_001256213.1:c.1800C>A | NP_001243142.1:p.Val600= | |
| NM_001256214.1:c.1806C>A | NP_001243143.1:p.Val602= | |
| NM_152296.4:c.1767C>A | NP_689509.1:p.Val589= | |
| XM_011526991.1:c.1677C>A | XP_011525293.1:p.Val559= | |
| NM_152296.5:c.1767C>A MANE Select | NP_689509.1:p.Val589= | |
| NM_001256214.2:c.1806C>A | NP_001243143.1:p.Val602= | |
| NM_001256213.2:c.1800C>A | NP_001243142.1:p.Val600= |