Canonical Allele Identifier: CA440620384

Gene:

Linked Data

• gnomAD v4: 4-102501229-A-G
• MyVariant Identifiers: chr4:g.103422386A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501229A>G , CM000666.2:g.102501229A>G	GRCh38
NC_000004.11:g.103422386A>G , CM000666.1:g.103422386A>G	GRCh37
NC_000004.10:g.103641418A>G	NCBI36
NG_050628.1:g.4901A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011532467.1:c.643+20T>C	XP_011530769.1:n.643+20T>C
NR_136202.1:n.48+1210T>C