Canonical Allele Identifier: CA270114145
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs944545746
MyVariant Identifiers: chr15:g.45003644G>C (hg19) chr15:g.44711446G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711446G>C , CM000677.2:g.44711446G>C GRCh38
NC_000015.9:g.45003644G>C , CM000677.1:g.45003644G>C GRCh37
NC_000015.8:g.42790936G>C NCBI36
NG_012920.1:g.4960G>C
NG_012920.2:g.4970G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+6G>C
Search 100 bp 5'
Search 100 bp 3'