Canonical Allele Identifier: CA2576180940
Gene: ZSWIM7 HGNC NCBI
TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1189707635

Genomic Alleles

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

Transcript Alleles

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