Canonical Allele Identifier: CA1216113071
Gene:

Linked Data

dbSNP Id: rs1572139044

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.193121705A>C , CM000663.2:g.193121705A>C GRCh38
NC_000001.10:g.193090835A>C , CM000663.1:g.193090835A>C GRCh37
NC_000001.9:g.191357458A>C NCBI36
NG_012691.1:g.4748A>C , LRG_507:g.4748A>C

Transcript Alleles

HGVS Amino-acid Change
XR_001738350.1:n.1952T>G