Canonical Allele Identifier: CA798374999

Gene:

Linked Data

• dbSNP Id: rs1291839333
• MyVariant Identifiers: chr4:g.74554066G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74554066G>T , CM000666.2:g.74554066G>T	GRCh38
NC_000004.11:g.75419783G>T , CM000666.1:g.75419783G>T	GRCh37
NC_000004.10:g.75638647G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741513.1:n.167-1234C>A