Canonical Allele Identifier: CA18888228

Gene:

Linked Data

• dbSNP Id: rs531388679
• MyVariant Identifiers: chr1:g.20200989C>G (hg19) ; chr1:g.19874496C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19874496C>G , CM000663.2:g.19874496C>G	GRCh38
NC_000001.10:g.20200989C>G , CM000663.1:g.20200989C>G	GRCh37
NC_000001.9:g.20073576C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_947027.1:n.266-8744G>C
XR_947028.1:n.266-8744G>C
XR_947027.2:n.167-8744G>C
XR_947028.2:n.167-8744G>C