Canonical Allele Identifier: CA1161925225
Gene:

Linked Data

dbSNP Id: rs1639363719

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523586G>C , CM000663.2:g.34523586G>C GRCh38
NC_000001.10:g.34989187G>C , CM000663.1:g.34989187G>C GRCh37
NC_000001.9:g.34761774G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947171.1:n.1073+23993C>G
XR_001737964.1:n.991+23993C>G