Canonical Allele Identifier: CA29957661

Gene: H2BC18

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149756186C>T , CM000663.2:g.149756186C>T	GRCh38
NC_000001.10:g.149727736C>T , CM000663.1:g.149727736C>T	GRCh37

Transcript Alleles

HGVS	Amino-acid Change
XM_006711337.2:c.*87G>A	XP_006711400.1:n.*87G>A