Canonical Allele Identifier: CA571437272

Gene: CCDC170

Linked Data

• dbSNP Id: rs1339204282
• gnomAD v2: 6-151936866-C-T
• gnomAD v4: 6-151615731-C-T
• MyVariant Identifiers: chr6:g.151936866C>T (hg19) ; chr6:g.151615731C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615731C>T , CM000668.2:g.151615731C>T	GRCh38
NC_000006.11:g.151936866C>T , CM000668.1:g.151936866C>T	GRCh37
NC_000006.10:g.151978559C>T	NCBI36
NG_021198.1:g.126692C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1947+52C>T MANE Select	ENSP00000239374.6:n.1947+52C>T
ENST00000239374.7:c.1947+52C>T	ENSP00000239374.6:n.1947+52C>T
NM_025059.3:c.1947+52C>T	NP_079335.2:n.1947+52C>T
XM_011536147.1:c.1965+52C>T	XP_011534449.1:n.1965+52C>T
XM_011536148.1:c.1764+52C>T	XP_011534450.1:n.1764+52C>T
XM_011536147.2:c.1965+52C>T	XP_011534449.1:n.1965+52C>T
XM_011536148.2:c.1764+52C>T	XP_011534450.1:n.1764+52C>T
XR_001743865.1:n.129+990G>A
NM_025059.4:c.1947+52C>T MANE Select	NP_079335.2:n.1947+52C>T