Canonical Allele Identifier: CA103120280
Gene:

Linked Data

dbSNP Id: rs1015484245
MyVariant Identifiers: chr4:g.102499845C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499845C>G , CM000666.2:g.102499845C>G GRCh38
NC_000004.11:g.103421002C>G , CM000666.1:g.103421002C>G GRCh37
NC_000004.10:g.103640034C>G NCBI36
NG_050628.1:g.3517C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1404G>C XP_011530769.1:n.643+1404G>C
NR_136202.1:n.48+2594G>C