Canonical Allele Identifier: CA2326044653
Gene: INSL3 HGNC NCBI

Linked Data

dbSNP Id: rs2094188326
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816766A>G , CM000681.2:g.17816766A>G GRCh38
NC_000019.9:g.17927575A>G , CM000681.1:g.17927575A>G GRCh37
NC_000019.8:g.17788575A>G NCBI36
NG_012092.1:g.9746T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.*88T>C MANE Select ENSP00000321724.6:n.*88T>C
ENST00000317306.7:c.*88T>C ENSP00000321724.6:n.*88T>C
ENST00000379695.5:c.*105T>C ENSP00000369017.4:n.*105T>C
ENST00000598577.1:c.505T>C
NM_001265587.1:c.*105T>C NP_001252516.1:n.*105T>C
NM_005543.3:c.*88T>C NP_005534.2:n.*88T>C
NM_001265587.2:c.*105T>C NP_001252516.1:n.*105T>C
NM_005543.4:c.*88T>C MANE Select NP_005534.2:n.*88T>C
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