Canonical Allele Identifier: CA798375024

Gene:

Linked Data

• dbSNP Id: rs1382550196
• MyVariant Identifiers: chr4:g.74554091G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74554091G>A , CM000666.2:g.74554091G>A	GRCh38
NC_000004.11:g.75419808G>A , CM000666.1:g.75419808G>A	GRCh37
NC_000004.10:g.75638672G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741513.1:n.167-1259C>T