Canonical Allele Identifier: CA10961801
Gene: PHGDH HGNC NCBI

Linked Data

dbSNP Id: rs1163251

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119667132T>C , CM000663.2:g.119667132T>C GRCh38
NC_000001.10:g.120209755T>C , CM000663.1:g.120209755T>C GRCh37
NC_000001.9:g.120011278T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641597.1:c.-615-2062T>C ENSP00000493382.1:n.-615-2062T>C
ENST00000493622.5:n.117-2059T>C