Canonical Allele Identifier: CA10605263

Gene: COL6A2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46112039T>C , CM000683.2:g.46112039T>C	GRCh38
NC_000021.8:g.47531953T>C , CM000683.1:g.47531953T>C	GRCh37
NC_000021.7:g.46356381T>C	NCBI36
NG_008675.1:g.18921T>C , LRG_476:g.18921T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.176T>C MANE Plus Clinical	ENSP00000380870.1:p.Met59Thr
ENST00000300527.9:c.176T>C MANE Select	ENSP00000300527.4:p.Met59Thr
ENST00000409416.6:c.176T>C	ENSP00000387115.1:p.Met59Thr
ENST00000300527.8:c.176T>C	ENSP00000300527.4:p.Met59Thr
ENST00000310645.9:c.176T>C	ENSP00000312529.5:p.Met59Thr
ENST00000397763.5:c.176T>C	ENSP00000380870.1:p.Met59Thr
ENST00000409416.5:c.176T>C	ENSP00000387115.1:p.Met59Thr
ENST00000436769.5:c.176T>C	ENSP00000390418.1:p.Met59Thr
NM_001849.3:c.176T>C , LRG_476t1:c.176T>C	NP_001840.3:p.Met59Thr
NM_058174.2:c.176T>C	NP_478054.2:p.Met59Thr
NM_058175.2:c.176T>C	NP_478055.2:p.Met59Thr
XM_011529451.1:c.176T>C	XP_011527753.1:p.Met59Thr
XM_011529452.1:c.176T>C	XP_011527754.1:p.Met59Thr
XR_937438.1:n.299T>C
XR_937439.1:n.299T>C
XR_937438.2:n.306T>C
XR_937439.2:n.306T>C
NM_001849.4:c.176T>C MANE Select	NP_001840.3:p.Met59Thr
NM_058174.3:c.176T>C MANE Plus Clinical	NP_478054.2:p.Met59Thr
NM_058175.3:c.176T>C	NP_478055.2:p.Met59Thr