Linked Data
dbSNP Id:
rs562931080
gnomAD v2:
16-31334249-C-T
gnomAD v3:
16-31322928-C-T
gnomAD v4:
16-31322928-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.31322928C>T , CM000678.2:g.31322928C>T | GRCh38 |
| NC_000016.9:g.31334249C>T , CM000678.1:g.31334249C>T | GRCh37 |
| NC_000016.8:g.31241750C>T | NCBI36 |
| NG_011719.1:g.67962C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000544665.9:c.2002+1301C>T MANE Select | ENSP00000441691.3:n.2002+1301C>T | |
| ENST00000648685.1:c.2005+1301C>T | ENSP00000496959.1:n.2005+1301C>T | |
| ENST00000287497.12:c.2002+1301C>T | ENSP00000287497.8:n.2002+1301C>T | |
| ENST00000544665.7:c.2005+1301C>T | ENSP00000441691.2:n.2005+1301C>T | |
| ENST00000567031.1:c.454-1471C>T | ||
| NM_000632.3:c.2002+1301C>T | NP_000623.2:n.2002+1301C>T | |
| NM_001145808.1:c.2005+1301C>T | NP_001139280.1:n.2005+1301C>T | |
| XM_011545850.1:c.1819+1301C>T | XP_011544152.1:n.1819+1301C>T | |
| XM_011545851.1:c.1842-1471C>T | XP_011544153.1:n.1842-1471C>T | |
| XR_950796.1:n.2095+1301C>T | ||
| XM_011545850.2:c.1819+1301C>T | XP_011544152.1:n.1819+1301C>T | |
| XM_011545851.2:c.1842-1471C>T | XP_011544153.1:n.1842-1471C>T | |
| XM_017023216.1:c.2005+1301C>T | XP_016878705.1:n.2005+1301C>T | |
| NM_000632.4:c.2002+1301C>T MANE Select | NP_000623.2:n.2002+1301C>T | |
| NM_001145808.2:c.2005+1301C>T | NP_001139280.1:n.2005+1301C>T |