Canonical Allele Identifier: CA773963153
Gene:

Linked Data

dbSNP Id: rs1218734519

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506431A>C , CM000679.2:g.63506431A>C GRCh38
NC_000017.10:g.61583792A>C , CM000679.1:g.61583792A>C GRCh37
NC_000017.9:g.58937524A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-625A>C ENSP00000464149.1:n.1970-625A>C