Canonical Allele Identifier: CA394884664

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16169747-C-A
• MyVariant Identifiers: chr16:g.16263604C>A (hg19) ; chr16:g.16169747C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169747C>A , CM000678.2:g.16169747C>A	GRCh38
NC_000016.9:g.16263604C>A , CM000678.1:g.16263604C>A	GRCh37
NC_000016.8:g.16171105C>A	NCBI36
NG_007558.2:g.58725G>T
NG_007558.3:g.58871G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2894G>T	ENSP00000483331.2:p.Gly965Val
ENST00000205557.12:c.2894G>T MANE Select	ENSP00000205557.7:p.Gly965Val
ENST00000205557.11:c.2894G>T	ENSP00000205557.7:p.Gly965Val
ENST00000456970.6:c.2719G>T	ENSP00000405002.2:n.2719G>T
ENST00000622290.4:c.*103G>T	ENSP00000483331.1:n.*103G>T
NM_001171.5:c.2894G>T	NP_001162.4:p.Gly965Val
XM_011522479.1:c.2861G>T	XP_011520781.1:p.Gly954Val
XM_011522480.1:c.2552G>T	XP_011520782.1:p.Gly851Val
XM_011522481.1:c.2552G>T	XP_011520783.1:p.Gly851Val
XR_932836.1:n.3129G>T
XR_932837.1:n.3130G>T
XR_932838.1:n.3130G>T
NM_001351800.1:c.2552G>T	NP_001338729.1:p.Gly851Val
NR_147784.1:n.2756G>T
XM_011522479.2:c.2861G>T	XP_011520781.1:p.Gly954Val
XM_011522481.3:c.2552G>T	XP_011520783.1:p.Gly851Val
XM_017023212.1:c.2726G>T	XP_016878701.1:p.Gly909Val
XM_017023214.1:c.2894G>T	XP_016878703.1:p.Gly965Val
XM_024450261.1:c.2930G>T	XP_024306029.1:p.Gly977Val
XR_932836.2:n.3075G>T
XR_932837.3:n.3075G>T
XR_932838.3:n.3075G>T
NM_001171.6:c.2894G>T MANE Select	NP_001162.5:p.Gly965Val