Canonical Allele Identifier: CA12264619
Gene: GPLD1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1883415

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24491247A>C , CM000668.2:g.24491247A>C GRCh38
NC_000006.11:g.24491475A>C , CM000668.1:g.24491475A>C GRCh37
NC_000006.10:g.24599454A>C NCBI36
NG_008161.1:g.1279A>C
NG_029888.2:g.3376T>G

Transcript Alleles

HGVS Amino-acid change
XM_011514509.1:c.45-1750T>G XP_011512811.1:p.=
XM_017010753.2:c.45-1750T>G XP_016866242.1:p.=
XR_002956277.1:n.267-1750T>G
ENST00000474784.5:n.240-1750T>G
ENST00000475417.1:n.234-1750T>G