Canonical Allele Identifier: CA501190700
Gene:

Linked Data

dbSNP Id: rs1170861903

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63498411C>T , CM000679.2:g.63498411C>T GRCh38
NC_000017.10:g.61575772C>T , CM000679.1:g.61575772C>T GRCh37
NC_000017.9:g.58929504C>T NCBI36
NG_011648.1:g.26339C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1969+1426C>T ENSP00000464149.1:n.1969+1426C>T