Canonical Allele Identifier: CA440618815

Gene:

Linked Data

• gnomAD v4: 4-102500884-G-T
• MyVariant Identifiers: chr4:g.103422041G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102500884G>T , CM000666.2:g.102500884G>T	GRCh38
NC_000004.11:g.103422041G>T , CM000666.1:g.103422041G>T	GRCh37
NC_000004.10:g.103641073G>T	NCBI36
NG_050628.1:g.4556G>T

Transcript Alleles

HGVS	Amino-acid Change
XM_011532467.1:c.643+365C>A	XP_011530769.1:n.643+365C>A
NR_136202.1:n.48+1555C>A