Canonical Allele Identifier: CA379105142
Gene: TNNI2 HGNC NCBI

Linked Data

gnomAD v4: 11-1840536-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840536G>T , CM000673.2:g.1840536G>T GRCh38
NC_000011.9:g.1861766G>T , CM000673.1:g.1861766G>T GRCh37
NC_000011.8:g.1818342G>T NCBI36
NG_011621.1:g.6534G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.66G>T MANE Select ENSP00000371336.1:p.Met22Ile
ENST00000252898.11:c.66G>T ENSP00000252898.7:p.Met22Ile
ENST00000381905.3:c.66G>T ENSP00000371330.3:p.Met22Ile
ENST00000381906.5:c.66G>T ENSP00000371331.1:p.Met22Ile
ENST00000381911.5:c.66G>T ENSP00000371336.1:p.Met22Ile
ENST00000468473.1:n.236G>T
ENST00000617947.4:c.66G>T ENSP00000481242.1:p.Met22Ile
NM_001145829.1:c.66G>T NP_001139301.1:p.Met22Ile
NM_001145841.1:c.66G>T NP_001139313.1:p.Met22Ile
NM_003282.3:c.66G>T NP_003273.1:p.Met22Ile
NM_003282.4:c.66G>T MANE Select NP_003273.1:p.Met22Ile
NM_001145829.2:c.66G>T NP_001139301.1:p.Met22Ile
NM_001145841.2:c.66G>T NP_001139313.1:p.Met22Ile