Canonical Allele Identifier: CA211665948
Gene:

Linked Data

dbSNP Id: rs889285961
MyVariant Identifiers: chr10:g.94762466C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762466C>T , CM000672.2:g.94762466C>T GRCh38
NC_000010.10:g.96522223C>T , CM000672.1:g.96522223C>T GRCh37
NC_000010.9:g.96512213C>T NCBI36
NG_008384.2:g.4761C>T
NG_008384.3:g.4786C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000464755.1:c.932-12592C>T ENSP00000483243.1:n.932-12592C>T