Canonical Allele Identifier: CA436215215

Gene: CP

Linked Data

• dbSNP Id: rs1559937992
• gnomAD v2: 3-148899868-G-A
• gnomAD v4: 3-149182081-G-A
• MyVariant Identifiers: chr3:g.148899868G>A (hg19) ; chr3:g.149182081G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182081G>A , CM000665.2:g.149182081G>A	GRCh38
NC_000003.11:g.148899868G>A , CM000665.1:g.148899868G>A	GRCh37
NC_000003.10:g.150382558G>A	NCBI36
NG_011800.1:g.44965C>T
NG_011800.2:g.44965C>T
NG_011800.3:g.44965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2478C>T MANE Select	ENSP00000264613.6:p.Asn826=
ENST00000264613.10:c.2478C>T	ENSP00000264613.6:p.Asn826=
ENST00000481169.5:c.2265C>T	ENSP00000418773.1:p.Asn755=
ENST00000490639.5:n.2510C>T
ENST00000494544.1:c.1827C>T	ENSP00000420545.1:p.Asn609=
NM_000096.3:c.2478C>T	NP_000087.1:p.Asn826=
NR_046371.1:n.2518C>T
XM_006713499.2:c.2478C>T	XP_006713562.1:p.Asn826=
XM_006713500.2:c.2478C>T	XP_006713563.1:p.Asn826=
XM_006713501.2:c.2478C>T	XP_006713564.1:p.Asn826=
XM_006713502.2:c.2478C>T	XP_006713565.1:p.Asn826=
XM_011512435.1:c.2478C>T	XP_011510737.1:p.Asn826=
XR_427361.2:n.2736C>T
XM_006713499.3:c.2478C>T	XP_006713562.1:p.Asn826=
XM_006713500.4:c.2478C>T	XP_006713563.1:p.Asn826=
XM_006713501.3:c.2478C>T	XP_006713564.1:p.Asn826=
XM_011512435.2:c.2478C>T	XP_011510737.1:p.Asn826=
XM_017005734.2:c.2478C>T	XP_016861223.1:p.Asn826=
XM_017005735.2:c.2478C>T	XP_016861224.1:p.Asn826=
XR_427361.3:n.2694C>T
NM_000096.4:c.2478C>T MANE Select	NP_000087.2:p.Asn826=
NR_046371.2:n.2302C>T