Canonical Allele Identifier: CA588310938

Gene: TMEM252-DT

Linked Data

• dbSNP Id: rs11143005
• gnomAD v2: 9-71193270-G-C
• gnomAD v3: 9-68578354-G-C
• gnomAD v4: 9-68578354-G-C
• MyVariant Identifiers: chr9:g.71193270G>C (hg19) ; chr9:g.68578354G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.68578354G>C , CM000671.2:g.68578354G>C	GRCh38
NC_000009.11:g.71193270G>C , CM000671.1:g.71193270G>C	GRCh37
NC_000009.10:g.70383090G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929903.1:n.449+35712G>C
XR_001746701.2:n.342+35712G>C