Canonical Allele Identifier: CA1138669511
Gene:

Linked Data

dbSNP Id: rs2051130280
gnomAD v3: Y-2800477-T-C
gnomAD v4: Y-2800477-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800477T>C , CM000686.2:g.2800477T>C GRCh38
NC_000024.9:g.2668518T>C , CM000686.1:g.2668518T>C GRCh37
NC_000024.8:g.2728518T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+25738T>C
ENST00000681787.1:n.106+25738T>C
ENST00000681940.1:n.106+25738T>C