Canonical Allele Identifier: CA1697903930
Gene:

Linked Data

dbSNP Id: rs1791159731

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911507C>T , CM000669.2:g.30911507C>T GRCh38
NC_000007.13:g.30951122C>T , CM000669.1:g.30951122C>T GRCh37
NC_000007.12:g.30917647C>T NCBI36
NG_007475.2:g.63114C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-486C>T