Canonical Allele Identifier: CA1163454629
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38168143C= , CM000663.2:g.38168143C= GRCh38
NC_000001.10:g.38633815C= , CM000663.1:g.38633815C= GRCh37
NC_000001.9:g.38406402C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947202.1:n.175+6320C=
XR_947203.1:n.62-24862C=
XR_947204.1:n.175+6320C=
XR_947205.1:n.175+6320C=
XR_001737984.1:n.175+6320C=
XR_001737985.1:n.62-24862C=
XR_001737986.1:n.175+6320C=
XR_001737987.1:n.175+6320C=
XR_002958294.1:n.175+6320C=
XR_947205.2:n.175+6320C=