Canonical Allele Identifier: CA2725530921
Gene:

Linked Data

dbSNP Id: rs2136673841

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6276622A>G , CM000674.2:g.6276622A>G GRCh38
NC_000012.11:g.6385788A>G , CM000674.1:g.6385788A>G GRCh37
NC_000012.10:g.6256049A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748976.1:n.157+16477T>C
XR_001748977.1:n.157+16477T>C
XR_001748978.1:n.157+16477T>C
XR_001748979.1:n.157+16477T>C
XR_001748980.1:n.157+16477T>C