Canonical Allele Identifier: CA464450837

Gene: RMRP

Linked Data

• dbSNP Id: rs1282617590
• gnomAD v4: 9-35657935-G-C
• MyVariant Identifiers: chr9:g.35657932G>C (hg19) ; chr9:g.35657935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35657935G>C , CM000671.2:g.35657935G>C	GRCh38
NC_000009.11:g.35657932G>C , CM000671.1:g.35657932G>C	GRCh37
NC_000009.10:g.35647932G>C	NCBI36
NG_017041.1:g.5084C>G , LRG_163:g.5084C>G
NG_033120.1:g.4646G>C

Transcript Alleles

HGVS	Amino-acid Change
NR_003051.3:n.84C>G , LRG_163t1:n.84C>G