Canonical Allele Identifier: CA371775893
Gene: POP1 HGNC NCBI

Linked Data

gnomAD v4: 8-98157816-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157816A>G , CM000670.2:g.98157816A>G GRCh38
NC_000008.10:g.99170044A>G , CM000670.1:g.99170044A>G GRCh37
NC_000008.9:g.99239220A>G NCBI36
NG_052869.1:g.45524A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000401707.7:c.2620A>G MANE Select ENSP00000385787.2:p.Met874Val
ENST00000349693.3:c.2620A>G ENSP00000339529.3:p.Met874Val
ENST00000401707.6:c.2620A>G ENSP00000385787.2:p.Met874Val
NM_001145860.1:c.2620A>G NP_001139332.1:p.Met874Val
NM_001145861.1:c.2620A>G NP_001139333.1:p.Met874Val
NM_015029.2:c.2620A>G NP_055844.2:p.Met874Val
NM_001145860.2:c.2620A>G MANE Select NP_001139332.1:p.Met874Val
NM_001145861.2:c.2620A>G NP_001139333.1:p.Met874Val
NM_015029.3:c.2620A>G NP_055844.2:p.Met874Val