Canonical Allele Identifier: CA37327618
Gene:

Linked Data

dbSNP Id: rs183861790

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682285A>G , CM000663.2:g.213682285A>G GRCh38
NC_000001.10:g.213855628A>G , CM000663.1:g.213855628A>G GRCh37
NC_000001.9:g.211922251A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738463.1:n.601-49132A>G
XR_001738464.1:n.426-49132A>G