Canonical Allele Identifier: CA404760780
Gene: INSL3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.17927754C>G (hg19) chr19:g.17816945C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17816945C>G , CM000681.2:g.17816945C>G GRCh38
NC_000019.9:g.17927754C>G , CM000681.1:g.17927754C>G GRCh37
NC_000019.8:g.17788754C>G NCBI36
NG_012092.1:g.9567G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000317306.8:c.305G>C MANE Select ENSP00000321724.6:p.Arg102Pro
ENST00000317306.7:c.305G>C ENSP00000321724.6:p.Arg102Pro
ENST00000379695.5:c.400G>C ENSP00000369017.4:p.Ala134Pro
ENST00000598577.1:c.326G>C
NM_001265587.1:c.400G>C NP_001252516.1:p.Ala134Pro
NM_005543.3:c.305G>C NP_005534.2:p.Arg102Pro
NM_001265587.2:c.400G>C NP_001252516.1:p.Ala134Pro
NM_005543.4:c.305G>C MANE Select NP_005534.2:p.Arg102Pro
Search 100 bp 5'
Search 100 bp 3'