Canonical Allele Identifier: CA2530105613
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2791270G>A , CM000686.2:g.2791270G>A GRCh38
NC_000024.9:g.2659311G>A , CM000686.1:g.2659311G>A GRCh37
NC_000024.8:g.2719311G>A NCBI36
NG_011751.1:g.1482C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+16531G>A
ENST00000681787.1:n.106+16531G>A
ENST00000681940.1:n.106+16531G>A