Canonical Allele Identifier: CA2628214444
Gene: B2M HGNC NCBI

Linked Data

gnomAD v4: 15-44711481-G-T
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000695792.1:n.83+41G>T
ENST00000558401.5:c.-66G>T ENSP00000452780.1:n.-66G>T
Search 100 bp 5'
Search 100 bp 3'