Canonical Allele Identifier: CA2173753322
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs1295629548
gnomAD v4: 15-44711484-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711484T>C , CM000677.2:g.44711484T>C GRCh38
NC_000015.9:g.45003682T>C , CM000677.1:g.45003682T>C GRCh37
NC_000015.8:g.42790974T>C NCBI36
NG_012920.1:g.4998T>C
NG_012920.2:g.5008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+44T>C
ENST00000558401.5:c.-63T>C ENSP00000452780.1:n.-63T>C
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