Canonical Allele Identifier: CA440619635
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422164G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501007G>C , CM000666.2:g.102501007G>C GRCh38
NC_000004.11:g.103422164G>C , CM000666.1:g.103422164G>C GRCh37
NC_000004.10:g.103641196G>C NCBI36
NG_050628.1:g.4679G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+242C>G XP_011530769.1:n.643+242C>G
NR_136202.1:n.48+1432C>G