Canonical Allele Identifier: CA440619910

Gene:

Linked Data

• gnomAD v4: 4-102501083-G-T
• MyVariant Identifiers: chr4:g.103422240G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102501083G>T , CM000666.2:g.102501083G>T	GRCh38
NC_000004.11:g.103422240G>T , CM000666.1:g.103422240G>T	GRCh37
NC_000004.10:g.103641272G>T	NCBI36
NG_050628.1:g.4755G>T

Transcript Alleles

HGVS	Amino-acid Change
XM_011532467.1:c.643+166C>A	XP_011530769.1:n.643+166C>A
NR_136202.1:n.48+1356C>A