Canonical Allele Identifier: CA14261888
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs12928822

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310036C>T , CM000678.2:g.11310036C>T GRCh38
NC_000016.9:g.11403893C>T , CM000678.1:g.11403893C>T GRCh37
NC_000016.8:g.11311394C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933070.1:n.733+60258C>T
XR_933070.3:n.876+60258C>T
ENST00000572173.1:c.-436-2793C>T ENSP00000461206.1:p.=
ENST00000573910.1:n.161-6416C>T