Canonical Allele Identifier: CA227396006
Gene: DYNC2H1 HGNC NCBI

Linked Data

dbSNP Id: rs183200281

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.103165845A>G , CM000673.2:g.103165845A>G GRCh38
NC_000011.9:g.103036574A>G , CM000673.1:g.103036574A>G GRCh37
NC_000011.8:g.102541784A>G NCBI36
NG_016423.1:g.61415A>G
NG_016423.2:g.61415A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000650373.2:c.4612-53A>G MANE Plus Clinical ENSP00000497174.1:n.4612-53A>G
ENST00000375735.7:c.4612-53A>G MANE Select ENSP00000364887.2:n.4612-53A>G
ENST00000649323.1:c.*2157-53A>G ENSP00000497581.1:n.*2157-53A>G
ENST00000650373.1:c.4612-53A>G ENSP00000497174.1:n.4612-53A>G
ENST00000334267.11:c.2205+31426A>G ENSP00000334021.7:n.2205+31426A>G
ENST00000375735.6:c.4612-53A>G ENSP00000364887.2:n.4612-53A>G
ENST00000398093.7:c.4612-53A>G ENSP00000381167.3:n.4612-53A>G
NM_001080463.1:c.4612-53A>G NP_001073932.1:n.4612-53A>G
NM_001377.2:c.4612-53A>G NP_001368.2:n.4612-53A>G
XM_006718903.2:c.4612-53A>G XP_006718966.1:n.4612-53A>G
XM_017018291.1:c.4612-53A>G XP_016873780.1:n.4612-53A>G
XM_017018292.1:c.3994-53A>G XP_016873781.1:n.3994-53A>G
XM_017018293.1:c.4612-53A>G XP_016873782.1:n.4612-53A>G
NM_001377.3:c.4612-53A>G MANE Select NP_001368.2:n.4612-53A>G
NM_001080463.2:c.4612-53A>G MANE Plus Clinical NP_001073932.1:n.4612-53A>G