Canonical Allele Identifier: CA92831165

Gene:

Linked Data

• dbSNP Id: rs970594779
• MyVariant Identifiers: chr4:g.11503649A>G (hg19) ; chr4:g.11502025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.11502025A>G , CM000666.2:g.11502025A>G	GRCh38
NC_000004.11:g.11503649A>G , CM000666.1:g.11503649A>G	GRCh37
NC_000004.10:g.11112747A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741361.1:n.950+19179A>G