Canonical Allele Identifier: CA2014002185
Gene:

Linked Data

dbSNP Id: rs1946882270

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276615T>C , CM000674.2:g.6276615T>C GRCh38
NC_000012.11:g.6385781T>C , CM000674.1:g.6385781T>C GRCh37
NC_000012.10:g.6256042T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748976.1:n.157+16484A>G
XR_001748977.1:n.157+16484A>G
XR_001748978.1:n.157+16484A>G
XR_001748979.1:n.157+16484A>G
XR_001748980.1:n.157+16484A>G