Canonical Allele Identifier: CA16398746
Gene:

Linked Data

dbSNP Id: rs3814637

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94761288C>T , CM000672.2:g.94761288C>T GRCh38
NC_000010.10:g.96521045C>T , CM000672.1:g.96521045C>T GRCh37
NC_000010.9:g.96511035C>T NCBI36
NG_008384.2:g.3583C>T
NG_008384.3:g.3608C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000464755.1:c.932-13770C>T ENSP00000483243.1:n.932-13770C>T