Canonical Allele Identifier: CA2647749540
Gene: H2BC21 HGNC NCBI

Linked Data

gnomAD v4: 1-149884421-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884421G>T , CM000663.2:g.149884421G>T GRCh38
NC_000001.10:g.149855971G>T , CM000663.1:g.149855971G>T GRCh37
NC_000001.9:g.148122595G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1843C>A ENSP00000375736.2:n.377+1843C>A
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