Canonical Allele Identifier: CA103120245
Gene:

Linked Data

dbSNP Id: rs1026896416
MyVariant Identifiers: chr4:g.102499649G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499649G>C , CM000666.2:g.102499649G>C GRCh38
NC_000004.11:g.103420806G>C , CM000666.1:g.103420806G>C GRCh37
NC_000004.10:g.103639838G>C NCBI36
NG_050628.1:g.3321G>C

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1600C>G XP_011530769.1:n.643+1600C>G
NR_136202.1:n.48+2790C>G