Canonical Allele Identifier: CA147641151

Gene: NCOA7

Linked Data

• dbSNP Id: rs1039734019
• MyVariant Identifiers: chr6:g.126153286C>G (hg19) ; chr6:g.125832140C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125832140C>G , CM000668.2:g.125832140C>G	GRCh38
NC_000006.11:g.126153286C>G , CM000668.1:g.126153286C>G	GRCh37
NC_000006.10:g.126194979C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392477.7:c.50+16736C>G MANE Select	ENSP00000376269.2:n.50+16736C>G
ENST00000229634.13:c.-42+16736C>G	ENSP00000229634.9:n.-42+16736C>G
ENST00000368357.7:c.50+16736C>G	ENSP00000357341.3:n.50+16736C>G
ENST00000392477.6:c.50+16736C>G	ENSP00000376269.2:n.50+16736C>G
ENST00000417494.5:c.50+16736C>G	ENSP00000406363.1:n.50+16736C>G
ENST00000419660.1:c.50+16736C>G	ENSP00000408211.1:n.50+16736C>G
ENST00000428318.1:c.50+16736C>G	ENSP00000407426.1:n.50+16736C>G
ENST00000453302.5:c.50+16736C>G	ENSP00000403643.1:n.50+16736C>G
ENST00000487635.1:n.187+16736C>G
NM_001122842.2:c.50+16736C>G	NP_001116314.1:n.50+16736C>G
NM_001199619.1:c.50+16736C>G	NP_001186548.1:n.50+16736C>G
NM_001199620.1:c.50+16736C>G	NP_001186549.1:n.50+16736C>G
NM_001199621.1:c.-42+16736C>G	NP_001186550.1:n.-42+16736C>G
NM_181782.4:c.50+16736C>G	NP_861447.3:n.50+16736C>G
XM_005266822.3:c.50+16736C>G	XP_005266879.1:n.50+16736C>G
XM_006715340.2:c.50+16736C>G	XP_006715403.1:n.50+16736C>G
XM_011535455.1:c.50+16736C>G	XP_011533757.1:n.50+16736C>G
XR_245505.1:n.419+16736C>G
XM_005266822.4:c.50+16736C>G	XP_005266879.1:n.50+16736C>G
XM_006715340.4:c.50+16736C>G	XP_006715403.1:n.50+16736C>G
XM_011535455.2:c.50+16736C>G	XP_011533757.1:n.50+16736C>G
XM_017010269.1:c.50+16736C>G	XP_016865758.1:n.50+16736C>G
XM_017010270.1:c.50+16736C>G	XP_016865759.1:n.50+16736C>G
XM_017010271.1:c.50+16736C>G	XP_016865760.1:n.50+16736C>G
XM_017010272.2:c.50+16736C>G	XP_016865761.1:n.50+16736C>G
XM_017010273.2:c.50+16736C>G	XP_016865762.1:n.50+16736C>G
XM_017010274.2:c.50+16736C>G	XP_016865763.1:n.50+16736C>G
XM_024446331.1:c.50+16736C>G	XP_024302099.1:n.50+16736C>G
XM_024446332.1:c.50+16736C>G	XP_024302100.1:n.50+16736C>G
XR_001743165.2:n.229+16736C>G
NM_181782.5:c.50+16736C>G MANE Select	NP_861447.3:n.50+16736C>G
NM_001122842.3:c.50+16736C>G	NP_001116314.1:n.50+16736C>G
NM_001199619.2:c.50+16736C>G	NP_001186548.1:n.50+16736C>G
NM_001199620.2:c.50+16736C>G	NP_001186549.1:n.50+16736C>G
NM_001199621.2:c.-42+16736C>G	NP_001186550.1:n.-42+16736C>G