Canonical Allele Identifier: CA307575998
Gene:

Linked Data

dbSNP Id: rs926536451
MyVariant Identifiers: chr19:g.34012913T>G (hg19) chr19:g.33522007T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33522007T>G , CM000681.2:g.33522007T>G GRCh38
NC_000019.9:g.34012913T>G , CM000681.1:g.34012913T>G GRCh37
NC_000019.8:g.38704753T>G NCBI36
NG_013358.1:g.4887A>C
NG_013358.2:g.4887A>C

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.66T>G
XR_935919.1:n.61T>G
XR_001754035.2:n.74T>G
XR_935918.2:n.74T>G
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