Canonical Allele Identifier: CA440618915
Gene:

Linked Data

MyVariant Identifiers: chr4:g.103422062T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500905T>G , CM000666.2:g.102500905T>G GRCh38
NC_000004.11:g.103422062T>G , CM000666.1:g.103422062T>G GRCh37
NC_000004.10:g.103641094T>G NCBI36
NG_050628.1:g.4577T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+344A>C XP_011530769.1:n.643+344A>C
NR_136202.1:n.48+1534A>C
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