Canonical Allele Identifier: CA1163450788
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.38158393T= , CM000663.2:g.38158393T= GRCh38
NC_000001.10:g.38624065T= , CM000663.1:g.38624065T= GRCh37
NC_000001.9:g.38396652T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947202.1:n.45-3300T=
XR_947203.1:n.61+16679T=
XR_947204.1:n.45-3300T=
XR_947205.1:n.45-3300T=
XR_001737984.1:n.45-3300T=
XR_001737985.1:n.61+16679T=
XR_001737986.1:n.45-3300T=
XR_001737987.1:n.45-3300T=
XR_002958294.1:n.45-3300T=
XR_947205.2:n.45-3300T=