Canonical Allele Identifier: CA4820869
Gene: POP1 HGNC NCBI

Linked Data

dbSNP Id: rs774510819
gnomAD v2: 8-99169954-G-T
gnomAD v4: 8-98157726-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157726G>T , CM000670.2:g.98157726G>T GRCh38
NC_000008.10:g.99169954G>T , CM000670.1:g.99169954G>T GRCh37
NC_000008.9:g.99239130G>T NCBI36
NG_052869.1:g.45434G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2530G>T MANE Select ENSP00000385787.2:p.Ala844Ser
ENST00000349693.3:c.2530G>T ENSP00000339529.3:p.Ala844Ser
ENST00000401707.6:c.2530G>T ENSP00000385787.2:p.Ala844Ser
NM_001145860.1:c.2530G>T NP_001139332.1:p.Ala844Ser
NM_001145861.1:c.2530G>T NP_001139333.1:p.Ala844Ser
NM_015029.2:c.2530G>T NP_055844.2:p.Ala844Ser
NM_001145860.2:c.2530G>T MANE Select NP_001139332.1:p.Ala844Ser
NM_001145861.2:c.2530G>T NP_001139333.1:p.Ala844Ser
NM_015029.3:c.2530G>T NP_055844.2:p.Ala844Ser