Canonical Allele Identifier: CA14408470
Gene:

Linked Data

dbSNP Id: rs16958990

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.66240275A>G , CM000679.2:g.66240275A>G GRCh38
NC_000017.10:g.64236393A>G , CM000679.1:g.64236393A>G GRCh37
NC_000017.9:g.61666855A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577982.1:c.-43-10853T>C ENSP00000464301.1:p.=