Canonical Allele Identifier: CA1644982421
Community Standard Title: NC_000006.12:g.88403098C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.88403098C= , CM000668.2:g.88403098C= GRCh38
NC_000006.11:g.89112817C= , CM000668.1:g.89112817C= GRCh37
NC_000006.10:g.89169536C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744248.2:n.330+38986G=
XR_001744250.1:n.321+38986G=
XR_001744251.1:n.321+38986G=
XR_001744252.2:n.321+38986G=
XR_001744253.1:n.394+38986G=
XR_942759.1:n.315+38986G=
XR_942759.2:n.321+38986G=
XR_942760.1:n.315+38986G=
XR_942761.1:n.315+38986G=
XR_942762.1:n.176+38986G=