Canonical Allele Identifier: CA2626329299
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94612263G>T , CM000676.2:g.94612263G>T GRCh38
NC_000014.8:g.95078600G>T , CM000676.1:g.95078600G>T GRCh37
NC_000014.7:g.94148353G>T NCBI36
NG_012879.1:g.4887G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000553947.1:c.805-34G>T