Canonical Allele Identifier: CA1303188208
Gene: GCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.162368011A>T , CM000664.2:g.162368011A>T GRCh38
NC_000002.11:g.163224521A>T , CM000664.1:g.163224521A>T GRCh37
NC_000002.10:g.162932767A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000414723.1:c.366-3295A>T
XM_005246446.2:c.628-3295A>T XP_005246503.1:n.628-3295A>T
XM_006712398.2:c.706-3295A>T XP_006712461.1:n.706-3295A>T
XM_006712399.2:c.705+8459A>T XP_006712462.1:n.705+8459A>T
XM_006712400.2:c.673-3295A>T XP_006712463.1:n.673-3295A>T
XM_011510926.1:c.571-3295A>T XP_011509228.1:n.571-3295A>T
XM_011510928.1:c.340-3295A>T XP_011509230.1:n.340-3295A>T
XM_005246446.3:c.628-3295A>T XP_005246503.1:n.628-3295A>T
XM_006712398.4:c.706-3295A>T XP_006712461.1:n.706-3295A>T
XM_006712400.4:c.673-3295A>T XP_006712463.1:n.673-3295A>T
XM_011510926.2:c.571-3295A>T XP_011509228.1:n.571-3295A>T
XM_011510928.2:c.340-3295A>T XP_011509230.1:n.340-3295A>T
XM_017003767.1:c.571-3295A>T XP_016859256.1:n.571-3295A>T