Canonical Allele Identifier: CA270114146
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs974572986
gnomAD v3: 15-44711455-G-A
gnomAD v4: 15-44711455-G-A
MyVariant Identifiers: chr15:g.45003653G>A (hg19) chr15:g.44711455G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711455G>A , CM000677.2:g.44711455G>A GRCh38
NC_000015.9:g.45003653G>A , CM000677.1:g.45003653G>A GRCh37
NC_000015.8:g.42790945G>A NCBI36
NG_012920.1:g.4969G>A
NG_012920.2:g.4979G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+15G>A
Search 100 bp 5'
Search 100 bp 3'