Canonical Allele Identifier: CA881156260
Gene:

Linked Data

dbSNP Id: rs1373053182
MyVariant Identifiers: chr19:g.29035392T>A (hg19) chr19:g.28544485T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544485T>A , CM000681.2:g.28544485T>A GRCh38
NC_000019.9:g.29035392T>A , CM000681.1:g.29035392T>A GRCh37
NC_000019.8:g.33727232T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-77705A>T
XR_243979.1:n.110-51462A>T
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