Canonical Allele Identifier: CA156094468
Gene:

Linked Data

dbSNP Id: rs576162886

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30897584A>G , CM000669.2:g.30897584A>G GRCh38
NC_000007.13:g.30937199A>G , CM000669.1:g.30937199A>G GRCh37
NC_000007.12:g.30903724A>G NCBI36
NG_007475.2:g.49191A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-14409A>G