Canonical Allele Identifier: CA29966198
Gene: H2BC21 HGNC NCBI

Linked Data

dbSNP Id: rs146252320
gnomAD v2: 1-149855922-C-T
gnomAD v3: 1-149884372-C-T
gnomAD v4: 1-149884372-C-T
MyVariant Identifiers: chr1:g.149855922C>T (hg19) chr1:g.149884372C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149884372C>T , CM000663.2:g.149884372C>T GRCh38
NC_000001.10:g.149855922C>T , CM000663.1:g.149855922C>T GRCh37
NC_000001.9:g.148122546C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369160.3:c.377+1892G>A ENSP00000375736.2:n.377+1892G>A
Search 100 bp 5'
Search 100 bp 3'