Canonical Allele Identifier: CA2160961156
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.104769221T= , CM000676.2:g.104769221T= GRCh38
NC_000014.8:g.105235558T= , CM000676.1:g.105235558T= GRCh37
NC_000014.7:g.104306603T= NCBI36
NG_012188.1:g.31524A= , LRG_721:g.31524A=

Transcript Alleles

HGVS Amino-acid Change
XR_429419.2:n.871T=
XR_429419.4:n.2106T=