Canonical Allele Identifier: CA307005696
Gene:

Linked Data

dbSNP Id: rs1018706652
gnomAD v3: 19-28544798-G-A
gnomAD v4: 19-28544798-G-A
MyVariant Identifiers: chr19:g.29035705G>A (hg19) chr19:g.28544798G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544798G>A , CM000681.2:g.28544798G>A GRCh38
NC_000019.9:g.29035705G>A , CM000681.1:g.29035705G>A GRCh37
NC_000019.8:g.33727545G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-78018C>T
XR_243979.1:n.110-51775C>T
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