Canonical Allele Identifier: CA1266819797
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545777C= , CM000664.2:g.85545777C= GRCh38
NC_000002.11:g.85772900C= , CM000664.1:g.85772900C= GRCh37
NC_000002.10:g.85626411C= NCBI36
NG_011811.2:g.20758G=
NG_029183.1:g.11800C=

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4157G= MANE Select ENSP00000233838.3:n.*4157G=
ENST00000233838.8:c.*4157G= ENSP00000233838.3:n.*4157G=
NM_000821.5:c.*4157G= NP_000812.2:n.*4157G=
NM_000821.6:c.*4157G= NP_000812.2:n.*4157G=
NM_001142269.2:c.*4157G= NP_001135741.1:n.*4157G=
NM_001142269.3:c.*4157G= NP_001135741.1:n.*4157G=
NM_000821.7:c.*4157G= MANE Select NP_000812.2:n.*4157G=
NM_001142269.4:c.*4157G= NP_001135741.1:n.*4157G=
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