Canonical Allele Identifier: CA2714349622
Gene:

Linked Data

dbSNP Id: rs2128587728

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30911417A>G , CM000669.2:g.30911417A>G GRCh38
NC_000007.13:g.30951032A>G , CM000669.1:g.30951032A>G GRCh37
NC_000007.12:g.30917557A>G NCBI36
NG_007475.2:g.63024A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509504.2:c.622-576A>G