Canonical Allele Identifier: CA156111423
Gene:

Linked Data

dbSNP Id: rs116667259
gnomAD v2: 7-30951065-G-A
gnomAD v3: 7-30911450-G-A
gnomAD v4: 7-30911450-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911450G>A , CM000669.2:g.30911450G>A GRCh38
NC_000007.13:g.30951065G>A , CM000669.1:g.30951065G>A GRCh37
NC_000007.12:g.30917590G>A NCBI36
NG_007475.2:g.63057G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000509504.2:c.622-543G>A