Canonical Allele Identifier: CA798354138

Gene:

Linked Data

• dbSNP Id: rs1249045681
• gnomAD v3: 4-74304339-A-G
• gnomAD v4: 4-74304339-A-G
• MyVariant Identifiers: chr4:g.75170056A>G (hg19) ; chr4:g.74304339A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74304339A>G , CM000666.2:g.74304339A>G	GRCh38
NC_000004.11:g.75170056A>G , CM000666.1:g.75170056A>G	GRCh37
NC_000004.10:g.75388920A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938877.1:n.120-25561T>C
XR_938877.2:n.126-25561T>C