Canonical Allele Identifier: CA439800876

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285248C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419531C>T , CM000666.2:g.73419531C>T	GRCh38
NC_000004.11:g.74285248C>T , CM000666.1:g.74285248C>T	GRCh37
NC_000004.10:g.74504112C>T	NCBI36
NG_009291.1:g.20277C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1677C>T MANE Select	ENSP00000295897.4:p.His559=
ENST00000295897.8:c.1677C>T	ENSP00000295897.4:p.His559=
ENST00000401494.7:c.1332C>T	ENSP00000384695.3:p.His444=
ENST00000415165.6:c.1101C>T	ENSP00000401820.2:p.His367=
ENST00000476441.6:c.*956C>T	ENSP00000423727.1:n.*956C>T
ENST00000486939.1:n.331C>T
ENST00000503124.5:c.1227C>T	ENSP00000421027.1:p.His409=
ENST00000505649.5:n.1224C>T
ENST00000508932.5:n.175+76C>T
ENST00000509063.5:c.1677C>T	ENSP00000422784.1:p.His559=
ENST00000511370.1:c.1210C>T
ENST00000621085.4:c.1038C>T	ENSP00000483421.1:p.His346=
ENST00000621628.4:c.1038C>T	ENSP00000480485.1:p.His346=
NM_000477.5:c.1677C>T	NP_000468.1:p.His559=
NM_000477.6:c.1677C>T	NP_000468.1:p.His559=
NM_000477.7:c.1677C>T MANE Select	NP_000468.1:p.His559=