Canonical Allele Identifier: CA624961112

Gene: ZSWIM7 TTC19

Linked Data

• dbSNP Id: rs768522330
• gnomAD v2: 17-15903003-C-A
• gnomAD v4: 17-15999689-C-A
• MyVariant Identifiers: chr17:g.15903003C>A (hg19) ; chr17:g.15999689C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999689C>A , CM000679.2:g.15999689C>A	GRCh38
NC_000017.10:g.15903003C>A , CM000679.1:g.15903003C>A	GRCh37
NC_000017.9:g.15843728C>A	NCBI36
NG_029806.1:g.5310C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399277.6:c.-95G>T (ZSWIM7) MANE Select	ENSP00000382218.1:n.-95G>T
ENST00000261647.9:c.-160C>A (TTC19)	ENSP00000261647.5:n.-160C>A
ENST00000399277.5:c.-95G>T (ZSWIM7)	ENSP00000382218.1:n.-95G>T
ENST00000399280.6:n.6G>T (ZSWIM7)
ENST00000491631.5:c.-95G>T (ZSWIM7)	ENSP00000462598.1:n.-95G>T
ENST00000497719.5:n.25G>T (ZSWIM7)
NM_001042697.1:c.-95G>T (ZSWIM7)	NP_001036162.1:n.-95G>T
NM_001042698.1:c.-95G>T (ZSWIM7)	NP_001036163.1:n.-95G>T
NM_001271420.1:c.-618C>A (TTC19)	NP_001258349.1:n.-618C>A
NM_017775.3:c.-160C>A (TTC19)	NP_060245.3:n.-160C>A
NM_001042697.2:c.-95G>T (ZSWIM7) MANE Select	NP_001036162.1:n.-95G>T
NM_001042698.2:c.-95G>T (ZSWIM7)	NP_001036163.1:n.-95G>T