Canonical Allele Identifier: CA357442372

Gene:

Linked Data

• dbSNP Id: rs558795443
• MyVariant Identifiers: chr4:g.75419910T>A (hg19) ; chr4:g.74554193T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74554193T>A , CM000666.2:g.74554193T>A	GRCh38
NC_000004.11:g.75419910T>A , CM000666.1:g.75419910T>A	GRCh37
NC_000004.10:g.75638774T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741513.1:n.167-1361A>T