Canonical Allele Identifier: CA18888187

Gene:

Linked Data

• dbSNP Id: rs895491049
• MyVariant Identifiers: chr1:g.20200958C>T (hg19) ; chr1:g.19874465C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19874465C>T , CM000663.2:g.19874465C>T	GRCh38
NC_000001.10:g.20200958C>T , CM000663.1:g.20200958C>T	GRCh37
NC_000001.9:g.20073545C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947027.1:n.266-8713G>A
XR_947028.1:n.266-8713G>A
XR_947027.2:n.167-8713G>A
XR_947028.2:n.167-8713G>A