Canonical Allele Identifier: CA182303321
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs995833573
gnomAD v3: 8-98158008-G-A
gnomAD v4: 8-98158008-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98158008G>A , CM000670.2:g.98158008G>A GRCh38
NC_000008.10:g.99170236G>A , CM000670.1:g.99170236G>A GRCh37
NC_000008.9:g.99239412G>A NCBI36
NG_052869.1:g.45716G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2812G>A MANE Select ENSP00000385787.2:p.Ala938Thr
ENST00000349693.3:c.2812G>A ENSP00000339529.3:p.Ala938Thr
ENST00000401707.6:c.2812G>A ENSP00000385787.2:p.Ala938Thr
NM_001145860.1:c.2812G>A NP_001139332.1:p.Ala938Thr
NM_001145861.1:c.2812G>A NP_001139333.1:p.Ala938Thr
NM_015029.2:c.2812G>A NP_055844.2:p.Ala938Thr
NM_001145860.2:c.2812G>A MANE Select NP_001139332.1:p.Ala938Thr
NM_001145861.2:c.2812G>A NP_001139333.1:p.Ala938Thr
NM_015029.3:c.2812G>A NP_055844.2:p.Ala938Thr