Canonical Allele Identifier: CA2661800322

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168906658T>C , CM000664.2:g.168906658T>C GRCh38
NC_000002.11:g.169763168T>C , CM000664.1:g.169763168T>C GRCh37
NC_000002.10:g.169471414T>C NCBI36
NG_011682.1:g.10419T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375363.8:c.441-6T>C (G6PC2) MANE Select ENSP00000364512.3:n.441-6T>C
ENST00000282075.5:c.*22-6T>C (G6PC2) ENSP00000282075.4:n.*22-6T>C
ENST00000375363.7:c.441-6T>C (G6PC2) ENSP00000364512.3:n.441-6T>C
ENST00000421979.1:c.219-910T>C (G6PC2) ENSP00000392183.1:n.219-910T>C
ENST00000429379.2:c.441-910T>C (G6PC2) ENSP00000396939.2:n.441-910T>C
ENST00000451987.5:c.-173+6542A>G (SPC25) ENSP00000393322.1:n.-173+6542A>G
ENST00000461586.1:n.157-910T>C (G6PC2)
ENST00000472216.2:n.176+6538A>G (SPC25)
NM_001081686.1:c.441-910T>C (G6PC2) NP_001075155.1:n.441-910T>C
NM_021176.2:c.441-6T>C (G6PC2) NP_066999.1:n.441-6T>C
XM_011511564.1:c.329-910T>C (G6PC2) XP_011509866.1:n.329-910T>C
XM_011511565.1:c.93-6T>C (G6PC2) XP_011509867.1:n.93-6T>C
XM_011511564.3:c.329-910T>C (G6PC2) XP_011509866.1:n.329-910T>C
XM_011511565.3:c.93-6T>C (G6PC2) XP_011509867.1:n.93-6T>C
NM_001081686.2:c.441-910T>C (G6PC2) NP_001075155.1:n.441-910T>C
NM_021176.3:c.441-6T>C (G6PC2) MANE Select NP_066999.1:n.441-6T>C