Canonical Allele Identifier: CA270114153
Gene: B2M HGNC NCBI

Linked Data

dbSNP Id: rs978737388
gnomAD v3: 15-44711483-G-C
gnomAD v4: 15-44711483-G-C
MyVariant Identifiers: chr15:g.45003681G>C (hg19) chr15:g.44711483G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44711483G>C , CM000677.2:g.44711483G>C GRCh38
NC_000015.9:g.45003681G>C , CM000677.1:g.45003681G>C GRCh37
NC_000015.8:g.42790973G>C NCBI36
NG_012920.1:g.4997G>C
NG_012920.2:g.5007G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+43G>C
ENST00000558401.5:c.-64G>C ENSP00000452780.1:n.-64G>C
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