Canonical Allele Identifier: CA1869965237
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.104928260G= , CM000671.2:g.104928260G= GRCh38
NC_000009.11:g.107690541G= , CM000671.1:g.107690541G= GRCh37
NC_000009.10:g.106730362G= NCBI36
NG_007981.1:g.4896C=

Transcript Alleles

HGVS Amino-acid change
XR_930204.1:n.734+350G=
XR_930204.2:n.115+350G=