Canonical Allele Identifier: CA1266822736
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547886T= , CM000664.2:g.85547886T= GRCh38
NC_000002.11:g.85775009T= , CM000664.1:g.85775009T= GRCh37
NC_000002.10:g.85628520T= NCBI36
NG_011811.2:g.18649A=

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2048A= MANE Select ENSP00000233838.3:n.*2048A=
ENST00000233838.8:c.*2048A= ENSP00000233838.3:n.*2048A=
ENST00000465637.5:n.297A=
NM_000821.5:c.*2048A= NP_000812.2:n.*2048A=
NM_000821.6:c.*2048A= NP_000812.2:n.*2048A=
NM_001142269.2:c.*2048A= NP_001135741.1:n.*2048A=
NM_001142269.3:c.*2048A= NP_001135741.1:n.*2048A=
NM_000821.7:c.*2048A= MANE Select NP_000812.2:n.*2048A=
NM_001142269.4:c.*2048A= NP_001135741.1:n.*2048A=