Canonical Allele Identifier: CA440619237

Gene:

Linked Data

• gnomAD v4: 4-102500976-G-C
• MyVariant Identifiers: chr4:g.103422133G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102500976G>C , CM000666.2:g.102500976G>C	GRCh38
NC_000004.11:g.103422133G>C , CM000666.1:g.103422133G>C	GRCh37
NC_000004.10:g.103641165G>C	NCBI36
NG_050628.1:g.4648G>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011532467.1:c.643+273C>G	XP_011530769.1:n.643+273C>G
NR_136202.1:n.48+1463C>G