Canonical Allele Identifier: CA886285247
Gene: PHGDH HGNC NCBI

Linked Data

dbSNP Id: rs1158726870

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119737406C>G , CM000663.2:g.119737406C>G GRCh38
NC_000001.10:g.120280029C>G , CM000663.1:g.120280029C>G GRCh37
NC_000001.9:g.120081552C>G NCBI36
NG_009188.1:g.30611C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369409.9:c.945+140C>G ENSP00000358417.5:n.945+140C>G
ENST00000641023.2:c.945+140C>G MANE Select ENSP00000493175.1:n.945+140C>G
ENST00000641074.1:c.945+140C>G ENSP00000493446.1:n.945+140C>G
ENST00000641115.1:c.945+140C>G ENSP00000493264.1:n.945+140C>G
ENST00000641213.1:c.*598+140C>G ENSP00000493079.1:n.*598+140C>G
ENST00000641314.1:n.930+140C>G
ENST00000641375.1:c.*781+140C>G ENSP00000493089.1:n.*781+140C>G
ENST00000641597.1:c.945+140C>G ENSP00000493382.1:n.945+140C>G
ENST00000641756.1:c.*689+140C>G ENSP00000493147.1:n.*689+140C>G
ENST00000641811.1:c.701+140C>G
ENST00000641891.1:c.*771+140C>G ENSP00000493288.1:n.*771+140C>G
ENST00000641927.1:n.885+140C>G
ENST00000641939.1:n.48+140C>G
ENST00000641947.1:c.945+140C>G ENSP00000492994.1:n.945+140C>G
ENST00000642021.1:n.1067+140C>G
ENST00000369407.3:c.843+140C>G ENSP00000358415.3:n.843+140C>G
ENST00000369409.8:c.945+140C>G ENSP00000358417.4:n.945+140C>G
NM_006623.3:c.945+140C>G NP_006614.2:n.945+140C>G
XM_011541226.1:c.1167+140C>G XP_011539528.1:n.1167+140C>G
XM_011541227.1:c.1089+140C>G XP_011539529.1:n.1089+140C>G
XM_011541228.1:c.1056+140C>G XP_011539530.1:n.1056+140C>G
XM_011541229.1:c.882+140C>G XP_011539531.1:n.882+140C>G
XM_011541230.1:c.660+140C>G XP_011539532.1:n.660+140C>G
XM_011541231.1:c.651+140C>G XP_011539533.1:n.651+140C>G
XM_011541226.2:c.1167+140C>G XP_011539528.1:n.1167+140C>G
XM_011541227.2:c.1089+140C>G XP_011539529.1:n.1089+140C>G
XM_011541228.2:c.1056+140C>G XP_011539530.1:n.1056+140C>G
XM_011541231.2:c.651+140C>G XP_011539533.1:n.651+140C>G
XM_024446338.1:c.1056+140C>G XP_024302106.1:n.1056+140C>G
NM_006623.4:c.945+140C>G MANE Select NP_006614.2:n.945+140C>G