Canonical Allele Identifier: CA12646688
Gene:

Linked Data

dbSNP Id: rs6945522
gnomAD v2: 7-30937235-C-T
gnomAD v3: 7-30897620-C-T
gnomAD v4: 7-30897620-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897620C>T , CM000669.2:g.30897620C>T GRCh38
NC_000007.13:g.30937235C>T , CM000669.1:g.30937235C>T GRCh37
NC_000007.12:g.30903760C>T NCBI36
NG_007475.2:g.49227C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000509504.2:c.622-14373C>T