Canonical Allele Identifier: CA31701871

Gene:

Linked Data

• dbSNP Id: rs192112744
• MyVariant Identifiers: chr1:g.168649504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649504C>G , CM000663.2:g.168649504C>G	GRCh38
NC_000001.10:g.168618742C>G , CM000663.1:g.168618742C>G	GRCh37
NC_000001.9:g.166885366C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8229G>C
XR_922259.2:n.332-8229G>C