Canonical Allele Identifier: CA542849122

Gene: GNAI2

Linked Data

• dbSNP Id: rs782108409
• gnomAD v2: 3-50293617-T-C
• gnomAD v3: 3-50256185-T-C
• gnomAD v4: 3-50256185-T-C
• MyVariant Identifiers: chr3:g.50293617T>C (hg19) ; chr3:g.50256185T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256185T>C , CM000665.2:g.50256185T>C	GRCh38
NC_000003.11:g.50293617T>C , CM000665.1:g.50293617T>C	GRCh37
NC_000003.10:g.50268621T>C	NCBI36
NG_016002.2:g.34498T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.465-7T>C MANE Select	ENSP00000312999.6:n.465-7T>C
ENST00000266027.9:c.309-7T>C	ENSP00000266027.6:n.309-7T>C
ENST00000313601.10:c.465-7T>C	ENSP00000312999.6:n.465-7T>C
ENST00000422163.5:c.417-7T>C	ENSP00000406871.1:n.417-7T>C
ENST00000440628.5:c.309-7T>C	ENSP00000395736.1:n.309-7T>C
ENST00000441156.5:c.422-7T>C	ENSP00000394321.1:n.422-7T>C
ENST00000446079.5:c.*100-7T>C	ENSP00000406065.1:n.*100-7T>C
ENST00000451956.1:c.354-7T>C	ENSP00000406369.1:n.354-7T>C
ENST00000468422.1:n.32-7T>C
ENST00000490122.5:n.1292-7T>C
ENST00000491100.5:n.2281-7T>C
NM_001166425.1:c.354-7T>C	NP_001159897.1:n.354-7T>C
NM_001282617.1:c.309-7T>C	NP_001269546.1:n.309-7T>C
NM_001282618.1:c.222-7T>C	NP_001269547.1:n.222-7T>C
NM_001282619.1:c.417-7T>C	NP_001269548.1:n.417-7T>C
NM_001282620.1:c.417-7T>C	NP_001269549.1:n.417-7T>C
NM_002070.3:c.465-7T>C	NP_002061.1:n.465-7T>C
NM_002070.4:c.465-7T>C MANE Select	NP_002061.1:n.465-7T>C
NM_001166425.2:c.354-7T>C	NP_001159897.1:n.354-7T>C
NM_001282618.2:c.222-7T>C	NP_001269547.1:n.222-7T>C
NM_001282619.2:c.417-7T>C	NP_001269548.1:n.417-7T>C
NM_001282620.2:c.417-7T>C	NP_001269549.1:n.417-7T>C
NM_001282617.2:c.309-7T>C	NP_001269546.1:n.309-7T>C