Canonical Allele Identifier: CA307575987
Gene:

Linked Data

dbSNP Id: rs536808217
gnomAD v3: 19-33521996-G-A
gnomAD v4: 19-33521996-G-A
MyVariant Identifiers: chr19:g.34012902G>A (hg19) chr19:g.33521996G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521996G>A , CM000681.2:g.33521996G>A GRCh38
NC_000019.9:g.34012902G>A , CM000681.1:g.34012902G>A GRCh37
NC_000019.8:g.38704742G>A NCBI36
NG_013358.1:g.4898C>T
NG_013358.2:g.4898C>T

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.55G>A
XR_935919.1:n.50G>A
XR_001754035.2:n.63G>A
XR_935918.2:n.63G>A
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