Canonical Allele Identifier: CA8262477
Gene: GEMIN4 HGNC NCBI

Linked Data

dbSNP Id: rs201006353
gnomAD v2: 17-649143-G-A
gnomAD v4: 17-745903-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.745903G>A , CM000679.2:g.745903G>A GRCh38
NC_000017.10:g.649143G>A , CM000679.1:g.649143G>A GRCh37
NC_000017.9:g.595893G>A NCBI36
NG_046938.1:g.11970C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000319004.6:c.2140C>T MANE Select ENSP00000321706.5:p.Leu714Phe
ENST00000319004.5:c.2140C>T ENSP00000321706.5:p.Leu714Phe
ENST00000576778.1:c.2107C>T ENSP00000459565.1:p.Leu703Phe
NM_015721.2:c.2140C>T NP_056536.2:p.Leu714Phe
XM_005256667.3:c.2152C>T XP_005256724.1:p.Leu718Phe
XM_005256668.3:c.2152C>T XP_005256725.1:p.Leu718Phe
XM_005256670.3:c.2107C>T XP_005256727.1:p.Leu703Phe
XM_011523910.1:c.2152C>T XP_011522212.1:p.Leu718Phe
XM_011523911.1:c.2152C>T XP_011522213.1:p.Leu718Phe
XM_011523912.1:c.2107C>T XP_011522214.1:p.Leu703Phe
XM_011523913.1:c.2107C>T XP_011522215.1:p.Leu703Phe
XM_005256667.4:c.2152C>T XP_005256724.1:p.Leu718Phe
XM_005256670.5:c.2107C>T XP_005256727.1:p.Leu703Phe
XM_011523910.2:c.2152C>T XP_011522212.1:p.Leu718Phe
XM_011523911.2:c.2152C>T XP_011522213.1:p.Leu718Phe
XM_011523912.2:c.2107C>T XP_011522214.1:p.Leu703Phe
XM_011523913.2:c.2107C>T XP_011522215.1:p.Leu703Phe
XM_017024709.1:c.2152C>T XP_016880198.1:p.Leu718Phe
NM_015721.3:c.2140C>T MANE Select NP_056536.2:p.Leu714Phe