Canonical Allele Identifier: CA1674890136
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817483G= , CM000668.2:g.155817483G= GRCh38
NC_000006.11:g.156138617G= , CM000668.1:g.156138617G= GRCh37
NC_000006.10:g.156180309G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24064G=
XR_943146.1:n.552-2813C=
XR_001744423.1:n.606-2813C=
XR_001744424.1:n.79+24064G=