Canonical Allele Identifier: CA1138669512
Gene:

Linked Data

dbSNP Id: rs757248803
gnomAD v3: Y-2800478-T-G
gnomAD v4: Y-2800478-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800478T>G , CM000686.2:g.2800478T>G GRCh38
NC_000024.9:g.2668519T>G , CM000686.1:g.2668519T>G GRCh37
NC_000024.8:g.2728519T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.106+25739T>G
ENST00000681787.1:n.106+25739T>G
ENST00000681940.1:n.106+25739T>G