Canonical Allele Identifier: CA192745660
Gene: RMRP HGNC NCBI

Linked Data

dbSNP Id: rs565037825
gnomAD v2: 9-35657935-C-T
gnomAD v3: 9-35657938-C-T
gnomAD v4: 9-35657938-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35657938C>T , CM000671.2:g.35657938C>T GRCh38
NC_000009.11:g.35657935C>T , CM000671.1:g.35657935C>T GRCh37
NC_000009.10:g.35647935C>T NCBI36
NG_017041.1:g.5081G>A , LRG_163:g.5081G>A
NG_033120.1:g.4649C>T

Transcript Alleles

HGVS Amino-acid Change
NR_003051.3:n.81G>A , LRG_163t1:n.81G>A