Canonical Allele Identifier: CA881625188
Gene:

Linked Data

dbSNP Id: rs40500
MyVariant Identifiers: chr19:g.34012861C>G (hg19) chr19:g.33521955C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521955C>G , CM000681.2:g.33521955C>G GRCh38
NC_000019.9:g.34012861C>G , CM000681.1:g.34012861C>G GRCh37
NC_000019.8:g.38704701C>G NCBI36
NG_013358.1:g.4939G>C
NG_013358.2:g.4939G>C

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.14C>G
XR_935919.1:n.9C>G
XR_001754035.2:n.22C>G
XR_935918.2:n.22C>G
Search 100 bp 5'
Search 100 bp 3'