Canonical Allele Identifier: CA2647749537
Gene: H2BC21 HGNC NCBI

Linked Data

gnomAD v4: 1-149884405-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884405G>T , CM000663.2:g.149884405G>T GRCh38
NC_000001.10:g.149855955G>T , CM000663.1:g.149855955G>T GRCh37
NC_000001.9:g.148122579G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1859C>A ENSP00000375736.2:n.377+1859C>A
Search 100 bp 5'
Search 100 bp 3'