Canonical Allele Identifier: CA881156474
Gene:

Linked Data

dbSNP Id: rs1321026913
gnomAD v3: 19-28544807-A-C
gnomAD v4: 19-28544807-A-C
MyVariant Identifiers: chr19:g.29035714A>C (hg19) chr19:g.28544807A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.28544807A>C , CM000681.2:g.28544807A>C GRCh38
NC_000019.9:g.29035714A>C , CM000681.1:g.29035714A>C GRCh37
NC_000019.8:g.33727554A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110759.1:n.657-78027T>G
XR_243979.1:n.110-51784T>G
Search 100 bp 5'
Search 100 bp 3'