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Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.91234409C= , CM000676.2:g.91234409C=
GRCh38
NC_000014.8:g.91700753C= , CM000676.1:g.91700753C=
GRCh37
NC_000014.7:g.90770506C=
NCBI36
NG_052988.1:g.24472G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000650645.1:c.642G=
MANE Select
ENSP00000498702.1:p.Arg214=
ENST00000529102.1:c.642G=
ENSP00000432740.1:p.Arg214=
ENST00000531499.2:c.642G=
ENSP00000434045.2:p.Arg214=
ENST00000535815.5:c.642G=
ENSP00000440797.1:p.Arg214=
NM_001177676.1:c.642G=
NP_001171147.1:p.Arg214=
NM_003485.3:c.642G=
NP_003476.3:p.Arg214=
XM_005268110.3:c.672G=
XP_005268167.1:p.Arg224=
XM_005268111.2:c.672G=
XP_005268168.1:p.Arg224=
XM_005268112.2:c.672G=
XP_005268169.1:p.Arg224=
XM_006720262.2:c.672G=
XP_006720325.1:p.Arg224=
XM_011537196.1:c.672G=
XP_011535498.1:p.Arg224=
XM_011537197.1:c.672G=
XP_011535499.1:p.Arg224=
XM_011537198.1:c.672G=
XP_011535500.1:p.Arg224=
XM_011537199.1:c.672G=
XP_011535501.1:p.Arg224=
XM_011537200.1:c.672G=
XP_011535502.1:p.Arg224=
NM_001348437.1:c.642G=
NP_001335366.1:p.Arg214=
XM_005268110.4:c.672G=
XP_005268167.1:p.Arg224=
XM_005268111.3:c.672G=
XP_005268168.1:p.Arg224=
XM_005268112.3:c.672G=
XP_005268169.1:p.Arg224=
XM_006720262.3:c.672G=
XP_006720325.1:p.Arg224=
XM_011537196.2:c.672G=
XP_011535498.1:p.Arg224=
XM_011537197.3:c.672G=
XP_011535499.1:p.Arg224=
XM_011537198.2:c.672G=
XP_011535500.1:p.Arg224=
XM_011537199.2:c.672G=
XP_011535501.1:p.Arg224=
NM_001177676.2:c.642G=
MANE Select
NP_001171147.1:p.Arg214=