Canonical Allele Identifier: CA2036556454
Gene: KRT74 HGNC NCBI

Linked Data

dbSNP Id: rs1939475896
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52571283A>G , CM000674.2:g.52571283A>G GRCh38
NC_000012.11:g.52965067A>G , CM000674.1:g.52965067A>G GRCh37
NC_000012.10:g.51251334A>G NCBI36
NG_012321.1:g.7543T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000305620.3:c.843+76T>C MANE Select ENSP00000307240.2:n.843+76T>C
ENST00000305620.2:c.843+76T>C ENSP00000307240.2:n.843+76T>C
ENST00000549343.5:c.843+76T>C ENSP00000447447.1:n.843+76T>C
NM_175053.3:c.843+76T>C NP_778223.2:n.843+76T>C
XM_011537902.1:c.843+76T>C XP_011536204.1:n.843+76T>C
NM_175053.4:c.843+76T>C MANE Select NP_778223.2:n.843+76T>C
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