Canonical Allele Identifier: CA1616896840

Linked Data

dbSNP Id: rs198846

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26107235A>C , CM000668.2:g.26107235A>C GRCh38
NC_000006.11:g.26107463A>C , CM000668.1:g.26107463A>C GRCh37
NC_000006.10:g.26215442A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000707188.1:c.391-16201T>G (H2BC4) ENSP00000516775.1:n.391-16201T>G
ENST00000629531.1:c.132+16538T>G (H2BC3) ENSP00000486472.1:n.132+16538T>G