Canonical Allele Identifier: CA156094476
Gene:

Linked Data

dbSNP Id: rs74326065
gnomAD v2: 7-30937200-C-T
gnomAD v3: 7-30897585-C-T
gnomAD v4: 7-30897585-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897585C>T , CM000669.2:g.30897585C>T GRCh38
NC_000007.13:g.30937200C>T , CM000669.1:g.30937200C>T GRCh37
NC_000007.12:g.30903725C>T NCBI36
NG_007475.2:g.49192C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14408C>T