dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.68249814G>T , CM000674.2:g.68249814G>T | GRCh38 |
| NC_000012.11:g.68643594G>T , CM000674.1:g.68643594G>T | GRCh37 |
| NC_000012.10:g.66929861G>T | NCBI36 |
| NG_060763.1:g.8791C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328087.6:c.463-938C>A | ENSP00000329384.4:n.463-938C>A | |
| ENST00000538666.6:c.463-938C>A MANE Select | ENSP00000442424.1:n.463-938C>A | |
| ENST00000328087.5:c.463-938C>A | ENSP00000329384.4:n.463-938C>A | |
| ENST00000538666.5:c.463-938C>A | ENSP00000442424.1:n.463-938C>A | |
| NM_020525.4:c.463-938C>A | NP_065386.1:n.463-938C>A | |
| XR_945055.1:n.265-14844G>T | ||
| NM_020525.5:c.463-938C>A MANE Select | NP_065386.1:n.463-938C>A | |
| XR_002957418.1:n.281-14844G>T |