Canonical Allele Identifier: CA464450995

Gene: RMRP

Linked Data

• ClinVar Variation Id: 1484735
• ClinVar RCV Id: RCV002006023
• dbSNP Id: rs1396054526
• gnomAD v2: 9-35657978-C-T
• gnomAD v3: 9-35657981-C-T
• gnomAD v4: 9-35657981-C-T
• MyVariant Identifiers: chr9:g.35657978C>T (hg19) ; chr9:g.35657981C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35657981C>T , CM000671.2:g.35657981C>T	GRCh38
NC_000009.11:g.35657978C>T , CM000671.1:g.35657978C>T	GRCh37
NC_000009.10:g.35647978C>T	NCBI36
NG_017041.1:g.5038G>A , LRG_163:g.5038G>A
NG_033120.1:g.4692C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_003051.3:n.38G>A , LRG_163t1:n.38G>A