Canonical Allele Identifier: CA1929213410
Gene:

Linked Data

dbSNP Id: rs1848183550

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762576A>C , CM000672.2:g.94762576A>C GRCh38
NC_000010.10:g.96522333A>C , CM000672.1:g.96522333A>C GRCh37
NC_000010.9:g.96512323A>C NCBI36
NG_008384.2:g.4871A>C
NG_008384.3:g.4896A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12482A>C ENSP00000483243.1:n.932-12482A>C