Canonical Allele Identifier: CA632705494
Gene:

Linked Data

dbSNP Id: rs1399770862
gnomAD v2: 19-34012901-C-A
gnomAD v3: 19-33521995-C-A
gnomAD v4: 19-33521995-C-A
MyVariant Identifiers: chr19:g.34012901C>A (hg19) chr19:g.33521995C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521995C>A , CM000681.2:g.33521995C>A GRCh38
NC_000019.9:g.34012901C>A , CM000681.1:g.34012901C>A GRCh37
NC_000019.8:g.38704741C>A NCBI36
NG_013358.1:g.4899G>T
NG_013358.2:g.4899G>T

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.54C>A
XR_935919.1:n.49C>A
XR_001754035.2:n.62C>A
XR_935918.2:n.62C>A
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