Canonical Allele Identifier: CA2647749521
Gene: H2BC21 HGNC NCBI

Linked Data

gnomAD v4: 1-149884347-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884347T>C , CM000663.2:g.149884347T>C GRCh38
NC_000001.10:g.149855897T>C , CM000663.1:g.149855897T>C GRCh37
NC_000001.9:g.148122521T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1917A>G ENSP00000375736.2:n.377+1917A>G
Search 100 bp 5'
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