Canonical Allele Identifier: CA270114150
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs921702518
gnomAD v2: 15-45003655-G-C
gnomAD v3: 15-44711457-G-C
gnomAD v4: 15-44711457-G-C
MyVariant Identifiers: chr15:g.45003655G>C (hg19) chr15:g.44711457G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711457G>C , CM000677.2:g.44711457G>C GRCh38
NC_000015.9:g.45003655G>C , CM000677.1:g.45003655G>C GRCh37
NC_000015.8:g.42790947G>C NCBI36
NG_012920.1:g.4971G>C
NG_012920.2:g.4981G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+17G>C
Search 100 bp 5'
Search 100 bp 3'