Canonical Allele Identifier: CA452133960
Gene: GJA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.121768593C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121447447C>T , CM000668.2:g.121447447C>T GRCh38
NC_000006.11:g.121768593C>T , CM000668.1:g.121768593C>T GRCh37
NC_000006.10:g.121810292C>T NCBI36
NG_008308.1:g.16849C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282561.4:c.600C>T MANE Select ENSP00000282561.3:p.Leu200=
ENST00000647564.1:c.600C>T ENSP00000497565.1:p.Leu200=
ENST00000649003.1:c.600C>T ENSP00000497283.1:p.Leu200=
ENST00000650427.1:c.600C>T ENSP00000497367.1:p.Leu200=
ENST00000282561.3:c.600C>T ENSP00000282561.3:p.Leu200=
NM_000165.4:c.600C>T NP_000156.1:p.Leu200=
NM_000165.5:c.600C>T MANE Select NP_000156.1:p.Leu200=