Canonical Allele Identifier: CA440619751
Gene:

Linked Data

dbSNP Id: rs2149087814
MyVariant Identifiers: chr4:g.103422193T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501036T>A , CM000666.2:g.102501036T>A GRCh38
NC_000004.11:g.103422193T>A , CM000666.1:g.103422193T>A GRCh37
NC_000004.10:g.103641225T>A NCBI36
NG_050628.1:g.4708T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+213A>T XP_011530769.1:n.643+213A>T
NR_136202.1:n.48+1403A>T
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