Canonical Allele Identifier: CA440619670

Gene:

Linked Data

• gnomAD v4: 4-102501018-G-A
• MyVariant Identifiers: chr4:g.103422175G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501018G>A , CM000666.2:g.102501018G>A	GRCh38
NC_000004.11:g.103422175G>A , CM000666.1:g.103422175G>A	GRCh37
NC_000004.10:g.103641207G>A	NCBI36
NG_050628.1:g.4690G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011532467.1:c.643+231C>T	XP_011530769.1:n.643+231C>T
NR_136202.1:n.48+1421C>T