Canonical Allele Identifier: CA2730858856
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs2141284145
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711481G>C , CM000677.2:g.44711481G>C GRCh38
NC_000015.9:g.45003679G>C , CM000677.1:g.45003679G>C GRCh37
NC_000015.8:g.42790971G>C NCBI36
NG_012920.1:g.4995G>C
NG_012920.2:g.5005G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+41G>C
ENST00000558401.5:c.-66G>C ENSP00000452780.1:n.-66G>C
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