Canonical Allele Identifier: CA59850212

Gene: G6PC2 SPC25

Linked Data

• dbSNP Id: rs970743466
• MyVariant Identifiers: chr2:g.169763059T>C (hg19) ; chr2:g.168906549T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168906549T>C , CM000664.2:g.168906549T>C	GRCh38
NC_000002.11:g.169763059T>C , CM000664.1:g.169763059T>C	GRCh37
NC_000002.10:g.169471305T>C	NCBI36
NG_011682.1:g.10310T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000375363.8:c.441-115T>C (G6PC2) MANE Select	ENSP00000364512.3:n.441-115T>C
ENST00000282075.5:c.*22-115T>C (G6PC2)	ENSP00000282075.4:n.*22-115T>C
ENST00000375363.7:c.441-115T>C (G6PC2)	ENSP00000364512.3:n.441-115T>C
ENST00000421979.1:c.219-1019T>C (G6PC2)	ENSP00000392183.1:n.219-1019T>C
ENST00000429379.2:c.441-1019T>C (G6PC2)	ENSP00000396939.2:n.441-1019T>C
ENST00000451987.5:c.-173+6651A>G (SPC25)	ENSP00000393322.1:n.-173+6651A>G
ENST00000461586.1:n.157-1019T>C (G6PC2)
ENST00000472216.2:n.176+6647A>G (SPC25)
NM_001081686.1:c.441-1019T>C (G6PC2)	NP_001075155.1:n.441-1019T>C
NM_021176.2:c.441-115T>C (G6PC2)	NP_066999.1:n.441-115T>C
XM_011511564.1:c.329-1019T>C (G6PC2)	XP_011509866.1:n.329-1019T>C
XM_011511565.1:c.93-115T>C (G6PC2)	XP_011509867.1:n.93-115T>C
XM_011511564.3:c.329-1019T>C (G6PC2)	XP_011509866.1:n.329-1019T>C
XM_011511565.3:c.93-115T>C (G6PC2)	XP_011509867.1:n.93-115T>C
NM_001081686.2:c.441-1019T>C (G6PC2)	NP_001075155.1:n.441-1019T>C
NM_021176.3:c.441-115T>C (G6PC2) MANE Select	NP_066999.1:n.441-115T>C