Canonical Allele Identifier: CA136260427

Linked Data

dbSNP Id: rs948911863

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107255G>T , CM000668.2:g.26107255G>T GRCh38
NC_000006.11:g.26107483G>T , CM000668.1:g.26107483G>T GRCh37
NC_000006.10:g.26215462G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16221C>A (H2BC4) ENSP00000516775.1:n.391-16221C>A
ENST00000629531.1:c.132+16518C>A (H2BC3) ENSP00000486472.1:n.132+16518C>A