Canonical Allele Identifier: CA270114151
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs967316673
gnomAD v3: 15-44711462-G-A
gnomAD v4: 15-44711462-G-A
MyVariant Identifiers: chr15:g.45003660G>A (hg19) chr15:g.44711462G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711462G>A , CM000677.2:g.44711462G>A GRCh38
NC_000015.9:g.45003660G>A , CM000677.1:g.45003660G>A GRCh37
NC_000015.8:g.42790952G>A NCBI36
NG_012920.1:g.4976G>A
NG_012920.2:g.4986G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+22G>A
Search 100 bp 5'
Search 100 bp 3'