Canonical Allele Identifier: CA10576148

Gene: PTGFR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.78490747T>C , CM000663.2:g.78490747T>C	GRCh38
NC_000001.10:g.78956432T>C , CM000663.1:g.78956432T>C	GRCh37
NC_000001.9:g.78729020T>C	NCBI36
NG_052997.1:g.4774T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370758.5:c.-72-1925T>C	ENSP00000359794.1:n.-72-1925T>C
XM_006710781.2:c.-72-1925T>C	XP_006710844.1:n.-72-1925T>C