Canonical Allele Identifier: CA624961114

Gene: ZSWIM7 TTC19

Linked Data

• dbSNP Id: rs1189707635
• gnomAD v2: 17-15903005-G-C
• gnomAD v4: 17-15999691-G-C
• MyVariant Identifiers: chr17:g.15903005G>C (hg19) ; chr17:g.15999691G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999691G>C , CM000679.2:g.15999691G>C	GRCh38
NC_000017.10:g.15903005G>C , CM000679.1:g.15903005G>C	GRCh37
NC_000017.9:g.15843730G>C	NCBI36
NG_029806.1:g.5312G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399277.6:c.-97C>G (ZSWIM7) MANE Select	ENSP00000382218.1:n.-97C>G
ENST00000261647.9:c.-158G>C (TTC19)	ENSP00000261647.5:n.-158G>C
ENST00000399277.5:c.-97C>G (ZSWIM7)	ENSP00000382218.1:n.-97C>G
ENST00000399280.6:n.4C>G (ZSWIM7)
ENST00000491631.5:c.-97C>G (ZSWIM7)	ENSP00000462598.1:n.-97C>G
ENST00000497719.5:n.23C>G (ZSWIM7)
NM_001042697.1:c.-97C>G (ZSWIM7)	NP_001036162.1:n.-97C>G
NM_001042698.1:c.-97C>G (ZSWIM7)	NP_001036163.1:n.-97C>G
NM_001271420.1:c.-616G>C (TTC19)	NP_001258349.1:n.-616G>C
NM_017775.3:c.-158G>C (TTC19)	NP_060245.3:n.-158G>C
NM_001042697.2:c.-97C>G (ZSWIM7) MANE Select	NP_001036162.1:n.-97C>G
NM_001042698.2:c.-97C>G (ZSWIM7)	NP_001036163.1:n.-97C>G