Canonical Allele Identifier: CA440618927
Gene:

Linked Data

gnomAD v4: 4-102500908-T-C
MyVariant Identifiers: chr4:g.103422065T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500908T>C , CM000666.2:g.102500908T>C GRCh38
NC_000004.11:g.103422065T>C , CM000666.1:g.103422065T>C GRCh37
NC_000004.10:g.103641097T>C NCBI36
NG_050628.1:g.4580T>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+341A>G XP_011530769.1:n.643+341A>G
NR_136202.1:n.48+1531A>G
Search 100 bp 5'
Search 100 bp 3'