Canonical Allele Identifier: CA14360409
Gene:

Linked Data

dbSNP Id: rs12446632
gnomAD v2: 16-19935389-G-A
gnomAD v3: 16-19924067-G-A
gnomAD v4: 16-19924067-G-A
MyVariant Identifiers: chr16:g.19935389G>A (hg19) chr16:g.19924067G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.19924067G>A , CM000678.2:g.19924067G>A GRCh38
NC_000016.9:g.19935389G>A , CM000678.1:g.19935389G>A GRCh37
NC_000016.8:g.19842890G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_950894.1:n.131+345G>A
XR_950894.2:n.121+345G>A
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Search 100 bp 3'